General Enantioselective C−H Activation with Efficiently Tunable Cyclopentadienyl Ligands

被引：0
|
作者：
Jia, Zhi-Jun [1 ,2 ]
Merten, Christian [3 ]
Gontla, Rajesh [1 ]
Daniliuc, Constantin G. [4 ]
Antonchick, Andrey P. [1 ,2 ]
Waldmann, Herbert [1 ,2 ]
机构：
[1] Max-Planck-Institut für Molekulare Physiologie, Abteilung Chemische Biologie, Otto-Hahn-Strasse 11, Dortmund,44227, Germany
[2] Technische Universität Dortmund, Fakultät Chemie und Chemische Biologie, Chemische Biologie, Otto-Hahn-Strasse 4a, Dortmund,44227, Germany
[3] Ruhr-Universität Bochum, Lehrstuhl für Organische Chemie II, Universitätsstrasse 150, Bochum,44801, Germany
[4] Westfälische Wilhelms-Universität Münster, Organisch-Chemisches Institut, Corrensstrasse 40, Münster,48149, Germany
来源：
Angewandte Chemie - International Edition | 2017年 / 56卷 / 09期
基金：
欧洲研究理事会;
关键词：
Compilation and indexing terms; Copyright 2024 Elsevier Inc;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
Asymmetric synthesis - Cycloadditions - Cyclopentadienyl ligands - Cyclopentadienyls - Enantioselective - Enantioselective transformation - Gram-scale synthesis - Structure variation
引用
收藏
页码：2429 / 2434
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